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Boron trifluoride → Ethyl 9-bromo-4-(hydroxymethyl)-4,5-dihydrobenzo[2,3]oxepino[4,5-d]thiazole-2-carboxylate

HRID 575294
ノート
印刷プレビュー

反応式

HRID 575294 の反応式
B(F)(F)F.[Br:5][C:6]1[CH:26]=[CH:25][C:9]2[O:10][CH2:11][C:12]3([C:15]4[S:19][C:18]([C:20]([O:22][CH2:23][CH3:24])=[O:21])=[N:17][C:16]=4[C:8]=2[CH:7]=1)[CH2:14][O:13]3.[SiH](CC)(CC)CC>ClCCl.C([O-])(O)=O.[Na+]>[Br:5][C:6]1[CH:26]=[CH:25][C:9]2[O:10][CH2:11][CH:12]([CH2:14][OH:13])[C:15]3[S:19][C:18]([C:20]([O:22][CH2:23][CH3:24])=[O:21])=[N:17][C:16]=3[C:8]=2[CH:7]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 6356Boron trifluorideHCID 12052TriethylsilaneHCID 86693323ethyl 9-bromo-5H-spiro[benzo[2,3]oxepino[4,5-d]thiazole-4,2'-oxirane]-2-carboxylate

生成物 1

HCID 86693325Ethyl 9-bromo-4-(hydroxymethyl)-4,5-dihydrobenzo[2,3]oxepino[4,5-d]thiazole-2-carboxylate収率 68%

試薬・触媒・溶媒 2

HCID 6344Dichloromethane溶媒
HCID 516892
Sodium Bicarbonate
溶媒

実験手順

Boron trifluoride diethleherate (0.16 mL, 1.00 equiv) was added dropwise to a stirred solution of ethyl 9-bromo-5H-spiro[benzo[2,3]oxepino[4,5-d]thiazole-4,2′-oxirane]-2-carboxylate (500 mg, 1.31 mmol, 1.00 equiv) and Et3SiH (227.5 mg, 1.96 mmol, 1.50 equiv) in dichloromethane (25 mL) at 0° C. After being stirred for 15 min at room temperature the reaction solution was diluted with 50 mL of aqueous NaHCO3, extracted with dichloromethane, dried over anhydrous sodium sulfate, and concentrated under vacuum. The residue was purified by a silica gel column with ethyl acetate/petroleum ether (1:3) to give 340 mg (68%) of the titled compound as a off-white solid; LC-MS (ES, m/z) 384,386 [M+H]+.

後処理

  1. extractionextracted with dichloromethane
  2. dry with materialdried over anhydrous sodium sulfate
  3. concentrationconcentrated under vacuum
  4. customThe residue was purified by a silica gel column with ethyl acetate/petroleum ether (1:3)

出典と根拠

ORDレコード
ord-599495e1caa74ad3a2a1bd7f48c36d73
出典データセット
uspto-grants-2015_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09034866B2

反応ノート

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